3',4'-DIHYDROXYPROPIOPHENONE
3',4'-DIHYDROXYPROPIOPHENONE Basic information
- Product Name:
- 3',4'-DIHYDROXYPROPIOPHENONE
- Synonyms:
-
- 1-(3,4-dihydroxyphenyl)-1-propanon
- 3’,4’-dihydroxy-propiophenon
- 3',4'-DIHYDROXYPROPIOPHENONE
- 3,4-DIHYDROXYPROPIOPHENONE
- 3',4'-Dihydroxypropiophenone,98%
- 2-[3-(hydroxymethyl)phenoxy]acetic acid
- 1-Propanone,1-(3,4-dihydroxyphenyl)-
- 1-(3,4-dihydroxyphenyl)propan-1-one
- CAS:
- 7451-98-1
- MF:
- C9H10O3
- MW:
- 166.17
- Product Categories:
-
- Aromatic Propiophenones (substituted)
- Mol File:
- 7451-98-1.mol
3',4'-DIHYDROXYPROPIOPHENONE Chemical Properties
- Melting point:
- 145-146°C
- Boiling point:
- 375.1±27.0 °C(Predicted)
- Density
- 1.237±0.06 g/cm3(Predicted)
- pka
- 8.75±0.31(Predicted)
- CAS DataBase Reference
- 7451-98-1(CAS DataBase Reference)
Safety Information
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
MSDS
- Language:English Provider:ALFA
3',4'-DIHYDROXYPROPIOPHENONE Usage And Synthesis
Uses
It is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.
Preparation
Obtained by Fries rearrangement of pyrocatechol dipropio-nate with aluminium chloride in chlorobenzene at 80° for 2 h (84%) or in nitrobenzene at 100° for 15 min;
Obtained by Fries rearrangement of pyrocatechol dipropionate with aluminium chloride in the presence of pyrocatechol, in nitrobenzene at 80° for 1 h (37%) or in nitromethane at r.t. for 72 h (76%)
Also obtained by Fries rearrangement of o-methoxyphenyl propionate (1 mol) by aluminium chloride (2 mol) without solvent at 140° for 2 h (51–55%) or in nitrobenzene at 80° for 30–60 min. A demethylation occurs during the reaction.
Also obtained by acylation of pyrocatechol with propionic acid
in the presence of boron trifluoride, at 150° for 2 h in a sealed tube ? (36%)
in the presence of polyphosphoric acid for 15 min in a boiling water bath ? (12%)
Preparation by demethylation of 4-hydroxy-3-methoxypropiophenone with refluxing pyridinium chloride for 10 min (80%)
Also obtained when propiovanillone was heated with an alkali sulfide under conditions used in the kraft cooking process.
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